(Q33480832)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Elizabeth Goldmuntz

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Marcin Imielinski

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Hakon Hakonarson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Tamim H Shaikh

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Xiaowu Gai

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Juan C Perin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Tracy Casalunovo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Laura K Conlin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Edward C Frackelton

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Kiran Annaiah

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Jonathan P Bradfield

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Andrew Eckert

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Chioma C Onyiah

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

George Otieno Ong'amo

object named as

F George Otieno

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Julie L Shaner

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Robert Skraban

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Nancy B Spinner

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Elaine H Zackai

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Rosetta M Chiavacci

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Robert Grundmeier

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Eric F Rappaport

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Kevin Murphy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Ryan O'Hara

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Elizabeth A Geiger

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Chad Haldeman-Englert

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Cecilia E Kim

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Livija Medne

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Elvira Dabaghyan

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Svetlana Ostapenko

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Erin Santa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Ryan M Smith

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Josephine Elia

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Peter S White

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

publication date

10 July 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

1682-1690

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

2 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Large recurrent microdeletions associated with schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Strong association of de novo copy number mutations with sporadic schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Mapping and sequencing of structural variation from eight human genomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

The fine-scale and complex architecture of human copy-number variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

A second generation human haplotype map of over 3.1 million SNPs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Genomic rearrangements and sporadic disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Strong association of de novo copy number mutations with autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

A comprehensive analysis of common copy-number variations in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Global variation in copy number in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Copy number variation: new insights in genome diversity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Structural variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Segmental duplications and copy-number variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Detection of large-scale variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Large-scale copy number polymorphism in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

The International HapMap Project

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Genomic microarrays in human genetic disease and cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Common deletion polymorphisms in the human genome.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Whole-genome genotyping with the single-base extension assay

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

A genome-wide scalable SNP genotyping assay using microarray technology

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

Common deletions and SNPs are in linkage disequilibrium in the human genome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752118

A high-resolution survey of deletion polymorphism in the human genome

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19592680

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1101/GR.083501.108

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

release_wyydwy7ejbaolleydrjvcgduaq

2 February 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wyydwy7ejbaolleydrjvcgduaq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

PubMed publication ID

19592680

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19592680%20AND%20SRC:MED&resulttype=core&format=json